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rs1998598

From SNPedia

Orientationplus
Stabilizedplus
Make rs1998598(A;A)
Make rs1998598(A;G)
Make rs1998598(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position197758512
GeneDENND1B
is asnp
is mentioned by
dbSNPrs1998598
ebirs1998598
HLIrs1998598
Exacrs1998598
Varsomers1998598
Maprs1998598
PheGenIrs1998598
hapmaprs1998598
1000 genomesrs1998598
hgdprs1998598
ensemblrs1998598
gopubmedrs1998598
geneviewrs1998598
scholarrs1998598
googlers1998598
pharmgkbrs1998598
gwascentralrs1998598
openSNPrs1998598
23andMers1998598
23andMe allrs1998598
SNP Nexus

SNPshotrs1998598
SNPdbers1998598
MSV3drs1998598
GWAS Ctlgrs1998598
GMAF0.225
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21102463OA-icon.png]
Trait
Title Genome-wide meta-analysis increases to 71 the number of confirmed Crohn's disease susceptibility loci
Risk Allele G
P-val 9E-9
Odds Ratio 1.0400 [1.00-1.09]